Canonical Allele Identifier: PA915961580
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12969
ClinVar Variation Id: 132992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001036188.1:p.Gly341Arg
CA023827
NM_001042723.2:c.1021G>A
CA023828
NM_001042723.2:c.1021G>C